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1
المؤلفون: Lijiang Ma, James F. Martin, Elizabeth A. Lindsay, Antonio Baldini, Fabiana Cerrato, Francesca Vitelli, Yasuhide Furuta, Huansheng Xu, Zhen Zhang, Masae Morishima, Joshua W. Vincentz
المساهمون: Zhang, Z, Cerrato, F, Xu, H, Vitelli, F, Morishima, M, Vincentz, J, Furuta, Y, Ma, L, Martin, J, Baldini, Antonio, Lindsay, E. A.
مصطلحات موضوعية: TBX1, Mesoderm, Pathology, medicine.medical_specialty, Gene Dosage, Aorta, Thoracic, Mice, Inbred Strains, Ectoderm, Biology, Epithelium, Mice, stomatognathic system, DiGeorge syndrome, Pharyngeal apparatus, medicine, Animals, Molecular Biology, Pharynx, Arteries, Anatomy, biochemical phenomena, metabolism, and nutrition, Embryo, Mammalian, medicine.disease, Branchial Region, medicine.anatomical_structure, embryonic structures, Endoderm, T-Box Domain Proteins, Gene Deletion, Pharyngeal arch, Developmental Biology
وصف الملف: STAMPA
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::756166440cb1f6a59dca30383d34f980Test
http://hdl.handle.net/11588/100147Test -
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المؤلفون: Antonio Baldini, Tiziano Pramparo, George Ogunrinu, Francesca Vitelli, Hong Su, Tuong Huynh, Vesna Jurecic, Masae Morishima, Helen F. Sutherland, Peter J. Scambler, Allan Bradley, Elizabeth A. Lindsay
المساهمون: Lindsay, E. A., Vitelli, F., Su, H., Morishima, M., Huynh, T., Pramparo, T., Jurecic, V., Ogunrinu, G., Sutherland, H., Scambler, P., Bradley, A., Baldini, Antonio
مصطلحات موضوعية: TBX1, Molecular Sequence Data, Aorta, Thoracic, Mice, Transgenic, Biology, Cell Line, Mice, 22q11 Deletion Syndrome, Pharyngeal apparatus, DiGeorge syndrome, medicine, DiGeorge Syndrome, Animals, Humans, Genetics, Multidisciplinary, medicine.disease, Mice, Inbred C57BL, medicine.anatomical_structure, Haplotypes, Mutagenesis, Aortic Arch Syndrome, Chromosomal region, Gene Targeting, Haploinsufficiency, T-Box Domain Proteins, Pharyngeal arch, Gene Deletion
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::696f5d08107b9bd3511be4b5d3b8fef8Test
http://hdl.handle.net/11386/2292347Test -
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المؤلفون: Francesca Vitelli, Marco Seri, Oscar Moran, Luis J. V. Galietta, Alessandra Renieri, Barbara R. Pober, Sandro Banfi, Alessandro Bulfone, Monica Piccini
المساهمون: Piccini, M, Vitelli, F, Seri, M, Galietta, Lj, Moran, O, Bulfone, A, Banfi, Sandro, Pober, B, Renieri, A., Piccini, Monica, Vitelli, Francesca, Seri, Marco, Galietta, Luis J. V., Moran, Oscar, Bulfone, Alessandro, Pober, Barbara, Renieri, Alessandra
المصدر: ResearcherID
مصطلحات موضوعية: Heart Defects, Congenital, Male, Potassium Channels, X Chromosome, Databases, Factual, Protein family, Molecular Sequence Data, Gene Expression, Nephritis, Hereditary, Contiguous gene syndrome, Homology (biology), Clone Cell, Electrocardiography, Mice, Intellectual Disability, Sequence Homology, Nucleic Acid, Gene expression, Genetics, medicine, Animals, Humans, Membrane Protein, Gene, In Situ Hybridization, Potassium Channel, biology, Animal, cDNA library, Electric Conductivity, Chromosome Mapping, Membrane Proteins, Syndrome, KCNE4, medicine.disease, Molecular biology, Clone Cells, Open reading frame, Potassium Channels, Voltage-Gated, biology.protein, Gene Deletion, Human
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8014257c85c4d6b06d92bb4283448808Test
http://hdl.handle.net/11591/217721Test -
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المؤلفون: Marcello Villanova, Massimo Zollo, Mirella Bruttini, Andrea Ballabio, Monica Piccini, Francesca Vitelli, Jon J. Jonsson, Giuseppe Borsani, Barbara R. Pober, Alessandra Renieri
المساهمون: Piccini, M, Vitelli, F, Bruttini, M, Pober, B. R., Jonsson, J. J., Villanova, M, Zollo, Massimo, Borsani, G, Ballabio, Andrea, Renieri, A.
مصطلحات موضوعية: Male, Saccharomyces cerevisiae Proteins, X Chromosome, Hereditary elliptocytosis, Molecular Sequence Data, Nephritis, Hereditary, Biology, ACSL4, Contiguous gene syndrome, Gene mapping, Intellectual Disability, Coenzyme A Ligases, Genetics, medicine, Humans, Amino Acid Sequence, Alport syndrome, Child, Gene, Gene map, Base Sequence, Alternative splicing, Elliptocytosis, Hereditary, Chromosome Mapping, medicine.disease, Repressor Proteins, Child, Preschool, Multigene Family, Gene Deletion
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aef4d6d0415fb0c096d9a9ccf961c801Test
http://hdl.handle.net/11379/5360Test